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Fragile X syndrome phenotype with normal FMR1 gene studies

2004; Wiley; Volume: 129A; Issue: 3 Linguagem: Inglês

10.1002/ajmg.a.30194

1552-4833

Nigel F. Clarke, David Mowat, R. Frank Kooy, Edwin Reyniers, Rob Willemsen,

Genomic variations and chromosomal abnormalities

American Journal of Medical Genetics Part AVolume 129A, Issue 3 p. 326-328 Research Letter Fragile X syndrome phenotype with normal FMR1 gene studies Nigel F. Clarke, Nigel F. Clarke Department of Medical Genetics, Sydney Children's Hospital and Department of Paediatrics, University of New South Wales, Sydney, AustraliaSearch for more papers by this authorDavid Mowat, Corresponding Author David Mowat d.mowat@unsw.edu.au Department of Medical Genetics, Sydney Children's Hospital and Department of Paediatrics, University of New South Wales, Sydney, AustraliaDepartment of Medical Genetics, Sydney Children's Hospital, High St, Randwick, Sydney, NSW 2031, Australia.Search for more papers by this authorR. Frank Kooy, R. Frank Kooy Department of Medical Genetics, University of Antwerp, Antwerp, BelgiumSearch for more papers by this authorEdwin Reyniers, Edwin Reyniers Department of Medical Genetics, University of Antwerp, Antwerp, BelgiumSearch for more papers by this authorRob Willemsen, Rob Willemsen Department of Clinical Genetics, Erasmus University, Rotterdam, The NetherlandsSearch for more papers by this author Nigel F. Clarke, Nigel F. Clarke Department of Medical Genetics, Sydney Children's Hospital and Department of Paediatrics, University of New South Wales, Sydney, AustraliaSearch for more papers by this authorDavid Mowat, Corresponding Author David Mowat d.mowat@unsw.edu.au Department of Medical Genetics, Sydney Children's Hospital and Department of Paediatrics, University of New South Wales, Sydney, AustraliaDepartment of Medical Genetics, Sydney Children's Hospital, High St, Randwick, Sydney, NSW 2031, Australia.Search for more papers by this authorR. Frank Kooy, R. Frank Kooy Department of Medical Genetics, University of Antwerp, Antwerp, BelgiumSearch for more papers by this authorEdwin Reyniers, Edwin Reyniers Department of Medical Genetics, University of Antwerp, Antwerp, BelgiumSearch for more papers by this authorRob Willemsen, Rob Willemsen Department of Clinical Genetics, Erasmus University, Rotterdam, The NetherlandsSearch for more papers by this author First published: 18 August 2004 https://doi.org/10.1002/ajmg.a.30194Citations: 1Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onFacebookTwitterLinked InRedditWechat Citing Literature Volume129A, Issue31 September 2004Pages 326-328 RelatedInformation